Stability Coordinator

What You’ll Do
- Coordinate with other departments to identify materials that need to be placed on stability.
- Author stability protocols and secure necessary approvals before each study begins.
- Review analytical data and compile it into a central database to support ongoing studies.
- Supply stability data needed for the submission of regulatory documents.
- Share stability data with other departments upon request.
- Maintain stability chamber inventory and monitor chamber performance.
- Remove samples from chambers according to protocol pull schedules and submit them to the appropriate testing group.
- Prepare samples for stability studies (aliquotting, labeling, and distributing to the correct chamber).
- Comply with all pertinent regulatory agency requirements, including Good Manufacturing Practice (GMP) standards.

Must-haves
- Bachelor’s degree in Life Sciences or a related field.
- Strong attention to detail and comfort working with data in a regulated environment.
- Ability to work independently and as part of a cross-functional team.
- Clear written and verbal communication skills, especially for authoring protocols and reporting data.

Preferred
- Prior experience in a stability program, quality control, or analytical testing environment.
- Familiarity with GMP or other regulated laboratory settings.
- Experience with database systems used to compile and track scientific data.
- Exposure to supporting regulatory submissions or interacting with regulatory agencies.

Benefits
- Student Loan Paydown program & Tuition Reimbursement
- Family Care Benefits
- Inclusion, Culture and Well-Being programs (including physical & mental health)

Application
- Apply now.